Canonical Allele Identifier: CA506424834
Gene: NCAN HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.19329836C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19219027C>A , CM000681.2:g.19219027C>A GRCh38
NC_000019.9:g.19329836C>A , CM000681.1:g.19329836C>A GRCh37
NC_000019.8:g.19190836C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252575.11:c.186C>A MANE Select ENSP00000252575.4:p.Thr62=
ENST00000252575.10:c.186C>A ENSP00000252575.4:p.Thr62=
NM_004386.2:c.186C>A NP_004377.2:p.Thr62=
XM_005259747.1:c.186C>A XP_005259804.1:p.Thr62=
NM_004386.3:c.186C>A MANE Select NP_004377.2:p.Thr62=
Search 100 bp 5'
Search 100 bp 3'